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Job Title: 0 - Evergreen, Supervisor, Production- Tablet Coating-...
Job Location: NJ: Kenilworth
Pay Rate: Open
Job Length: full time
Start Date: 2008-07-23

Company Name: Schering-Plough
Contact: HR
Phone: email only please
Fax: email only please

Description: Position Title 0 - Evergreen, Supervisor, Production- Tablet Coating- Midnight Business Division Global Supply Chain Country U.S.A. Location NJ Kenilworth Job Description Available shifts: Midnight - Kenilworth, NJ Schering-Plough is a global science-based health care company with leading prescription, consumer and animal health products. Through internal research and collaborations with partners, Schering-Plough discovers, develops, manufactures and markets advanced drug therapies to meet important medical needs. Schering-Plough’s vision is to earn the trust of the physicians, patients and customers served by its more than 50,000 people around the world. Schering-Plough is committed to attract and retain a diverse population of top professional talent worldwide. In order to remain in line with the companys fast-paced growth and expansion, we are moving towards a proactive solution of building relationships with qualified candidates for positions across our organization, often, before a need arises. This generic job description provides details on the profile of candidates that we want to engage to discuss current and/or similar future openings within our organization. We are seeking high-caliber candidates that will thrive in Schering-Plough’s diverse and innovative culture and will only contact those candidates who fit this profile. Responsible for the direct supervision of all departmental operations within Tablet Manufacturing area in accordance with approved procedures. Responsibilities:

* Operates all areas in compliance with all regulations and attempts to meet the production financial standards. * Supervises approximately 6 – 12 pharmaceutical operators plus support staff including mechanics, material handlers, porters and maintenance personnel. * Supervise, coordinate, and implement the daily operations. * Compliance with safety guidelines * Supervise, and perform as needed, all manufacturing operations * Observe Good Manufacturing practices while working around all products including, but not limited to proper documentation, training, gowning, etc. * Support or supervise process control and optimization programs * Supervise, and perform as needed, the creation and revision of production documents in order to maintain cGMP compliance and efficiency * Supervise, and perform as needed, employee training in manufacturing support and manufacturing operations * Responsible for the training monitoring and correcting of any deficiencies related to their direct reports. * Reports to the Pharmaceutical Manufacturing Manager and provides process and control improvement ideas and solutions for management evaluation. * Follow all safety rules and regulations. * Work with and assist production personnel as required to improve productivity and efficiency. * Submit GMP documentation, such as, Change Authorization (CA), Notice of Events (NOE), Corrective Actions / Preventive Actions (CAPA), Request For Concurrence (RFCs), etc. Minimal education required for this job Bachelor of Science Skills * Bachelors Degree in Engineering or Science. * Must possess 3-5 years experience in the pharmaceutical industry. * Must have at least 1 year experience supervising manufacturing production preferably within the pharmaceutical industry * Must have a thorough understanding of cGMP requirements for manufacturing facility. * Basic Engineering and Science knowledge Problem Solving, Root Cause, Verification. * Leadership skills: Provide direction, lead courageously, influence others, foster teamwork, motivate, coach and develop, champion change. * Thinking Skills: Analyze issues, use sound judgment and think strategically. * In-depth knowledge of the regulatory requirements (FDA, cGMPs, etc.) for pharmaceutical Manufacturing operations * Experience with equipment such as mixers - must have tablet presses, capsule, fluid beds and tablet coaters . * Thorough understanding of the documentation and change control processes * Effective management skills in interacting with cross-functional departments (Warehousing, Packaging, QA, QC, etc.) * Administrative skills: Establish Plans, Structure and Staff, Develop Systems and Processes, Manage execution and Work Efficiently. * Communication skills: Speak Effectively, Foster open communication, listen to others, and prepare written communication. * Organization Knowledge: Use technical/functional expertise and know the business. * Organization Strategy Skills: Commitment to Quality, focus on customer (internal) needs. * Self-Management Skills: Act with Integrity, Demonstrate adaptability and develop oneself. Employment Type Regular Full- or Part-Time Full-Time Work Schedule Night Requisition I.D. 21077BR

Please refer to Job code schering-819428 when responding to this ad.

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